GOOD SENSE PAIN RELIEF ROLL ON- lidocaine hcl liquid

Good Sense Pain Relief Roll On by

Drug Labeling and Warnings

Good Sense Pain Relief Roll On by is a Otc medication manufactured, distributed, or labeled by Geiss, Destin & Dunn, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Lidocaine HCl 4%

PURPOSE

Topical anesthetic

DOSAGE & ADMINISTRATION

For the temporary relief of pain and itching due to sunburn, minor burns, insect bites, minor cuts, scrapes, and minor skin irritations.

INDICATIONS & USAGE

For the temporary relief of pain

WARNINGS

For external use only.

Flammable. Keep away from excessive heat or open flame.

Do not use in large quantities, particularly over raw surfaces or blistered areas.

When using this product avoid contact with eyes. Rinse with water if contact occurs. Do not apply to wounds or damaged skin. Do not bandage tightly.

Stop use and ask a doctor if the condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days, and redness or irritation develops.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If the product is swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT

Acrylates/C10-30 alkyl acrylate crosspolymer, alcohol denat., aloe barbadensis leaf extract, aminomethyl propanol, C30-45 alkyl cetearyl dimethicone crosspolymer, caprylyl methicone, cetearyl alcohol, ceteth-20 phosphate, dicetyl phosphate, dimethicone, disodium EDTA, ethylhexylglycerin, glycerin stearate, methylparaben, steareth-21, water.

PREGNANCY OR BREAST FEEDING

Ask a health professional before use.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GOOD SENSE PAIN RELIEF ROLL ON 
lidocaine hcl liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50804-187
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	4 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
ALCOHOL (UNII: 3K9958V90M)
AMINOMETHYL PROPANOL (UNII: LU49E6626Q)
C30-45 ALKYL CETEARYL DIMETHICONE CROSSPOLYMER (UNII: 4ZK9VP326R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
CETETH-20 PHOSPHATE (UNII: 921FTA1500)
DICETYL PHOSPHATE (UNII: 2V6E5WN99N)
DIMETHICONE 200 (UNII: RGS4T2AS00)
EDETATE DISODIUM (UNII: 7FLD91C86K)
STEARETH-21 (UNII: 53J3F32P58)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
METHYLPARABEN (UNII: A2I8C7HI9T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50804-187-02	71 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/27/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	12/04/2020

Labeler - Geiss, Destin & Dunn, Inc (076059836)